Now hiring

Associate Director CMC Regulatory @ Actalent

Philadelphia, Pennsylvania, USOnsiteContract
Apply with ResuMinder

Opens on the employer's site

About this role

Embrace the role of an Associate Director, CMC Regulatory and lead regulatory affairs for innovative therapies, including gene therapies and biologics. Collaborate with clinical research teams, support FDA submissions, and drive regulatory strategy in a dynamic academic medical environment. Shape the future of clinical research and make a significant impact on patient outcomes.. Category: Clinical

Skills

regulatory submissionsfda clinical trial regulationsgmpglpind submissionsgvpgcpide submissionsregulatory documentationregulatory strategyanimal study supportprotocol developmentclinical trial protocolsregulatory writingstakeholder communication

Ready to apply?

Install the ResuMinder extension and we'll auto-fill the application in seconds — no rewriting.

See how your CV scores